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C21H18FNO5S

Base Information
  • Chemical Name:C21H18FNO5S
  • CAS No.:1374232-98-0
  • Molecular Formula:C21H18FNO5S
  • Molecular Weight:415.442
  • Hs Code.:
C<sub>21</sub>H<sub>18</sub>FNO<sub>5</sub>S

Synonyms:C21H18FNO5S

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Chemical Property of C21H18FNO5S
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Technology Process of C21H18FNO5S

There total 12 articles about C21H18FNO5S which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
C22H20FNO5S; With lithium hydroxide; In tetrahydrofuran; methanol; at 70 ℃; for 2h;
With hydrogenchloride; In tetrahydrofuran; methanol; water; at 20 ℃;
Guidance literature:
Multi-step reaction with 12 steps
1.1: copper(l) iodide; copper diacetate / water / 48 h / 100 °C
2.1: polyphosphoric acid / 3 h / 90 °C
3.1: triethylamine / dichloromethane / 3 h / 0 - 20 °C
4.1: n-butyllithium / tetrahydrofuran; hexane / 2 h / 0 °C
4.2: 0 - 20 °C
5.1: diethylzinc / hexane; toluene / 0 - 20 °C
6.1: N-Bromosuccinimide / dichloromethane / 1 h / 0 - 20 °C
7.1: boron tribromide / dichloromethane / 1 h / -20 - 0 °C
7.2: Cooling with ice
8.1: triethylamine / dmap / tetrahydrofuran / 10 h / 0 - 20 °C
9.1: piperidine / bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine / N,N-dimethyl-formamide / 80 °C / Inert atmosphere
10.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C
11.1: sodium acetate; potassium carbonate / copper dichloride; palladium dichloride / 20 °C
12.1: lithium hydroxide / tetrahydrofuran; methanol / 2 h / 70 °C
12.2: 20 °C
With piperidine; hydrogenchloride; N-Bromosuccinimide; n-butyllithium; diethylzinc; sodium acetate; boron tribromide; potassium carbonate; triethylamine; lithium hydroxide; dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine; copper diacetate; copper dichloride; palladium dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; toluene;
Guidance literature:
Multi-step reaction with 10 steps
1.1: triethylamine / dichloromethane / 3 h / 0 - 20 °C
2.1: n-butyllithium / tetrahydrofuran; hexane / 2 h / 0 °C
2.2: 0 - 20 °C
3.1: diethylzinc / hexane; toluene / 0 - 20 °C
4.1: N-Bromosuccinimide / dichloromethane / 1 h / 0 - 20 °C
5.1: boron tribromide / dichloromethane / 1 h / -20 - 0 °C
5.2: Cooling with ice
6.1: triethylamine / dmap / tetrahydrofuran / 10 h / 0 - 20 °C
7.1: piperidine / bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine / N,N-dimethyl-formamide / 80 °C / Inert atmosphere
8.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C
9.1: sodium acetate; potassium carbonate / copper dichloride; palladium dichloride / 20 °C
10.1: lithium hydroxide / tetrahydrofuran; methanol / 2 h / 70 °C
10.2: 20 °C
With piperidine; hydrogenchloride; N-Bromosuccinimide; n-butyllithium; diethylzinc; sodium acetate; boron tribromide; potassium carbonate; triethylamine; lithium hydroxide; dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tri-tert-butyl phosphine; copper dichloride; palladium dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; hexane; dichloromethane; N,N-dimethyl-formamide; toluene;
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